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J Comput Chem ; 37(12): 1068-81, 2016 May 05.
Artículo en Inglés | MEDLINE | ID: mdl-26833740

RESUMEN

Caryolene formation occur asynchronously in a concerted way through carbocationic rearrangements involving the generation of a secondary or a tertiary carbocation whether the reaction proceeds in the absence or in the presence of NH3 , respectively. Both caryolene formation mechanisms are analyzed within the general framework of the reaction force; the reaction force constant is used to gain insights into the synchronicity of the mechanisms and the reaction electronic flux helps to characterize the electronic activity taking place during the reaction. DFT calculations at the B3LYP/6-31+G(d,p) level show a clear difference in the mechanisms of the base promoted or base free caryolene formation reactions.


Asunto(s)
Amoníaco/química , Teoría Cuántica , Catálisis
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